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- source_evidence_literature type ECO_0000212 NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_provenance.
- NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_assertion description "[Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_provenance.
- NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_assertion evidence source_evidence_literature NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_provenance.
- NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_assertion SIO_000772 20736978 NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_provenance.
- NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_assertion wasDerivedFrom befree-20150227 NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_provenance.
- NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_assertion wasGeneratedBy ECO_0000203 NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP404346.RAJnXWM9j_C5av0T8Ja6IoSFLVqwxSgH0yponvZS0fydE130_provenance.